University of Arizona 2006
From 2006.igem.org
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Next Meeting: Mon 7/10 in Shantz 440 at 5:00 pm | Next Meeting: Mon 7/10 in Shantz 440 at 5:00 pm | ||
Revision as of 21:27, 4 October 2006
University of Arizona 2006
Contents |
Team
The Cell Raisers
"Splice Guys Finish First"
| Member | Contact | Role | |
|---|---|---|---|
| Joan Curry | curry@ag.arizona.edu | Faculty Advisor | |
| Mark Riley | riley@ag.arizona.edu | Faculty Advisor | |
| Patrick Hollinger | dogmod@email.arizona.edu | Lab Lead / Design | |
| Josh Kittleson | jkittles@email.arizona.edu | Lab work, Design | |
| Tim Spriggs | tims@u.arizona.edu | Project Manager / Documentation | |
| Tyler Brown | tylerb@email.arizona.edu | Documentation | |
| Dan Reavis | danman1@email.arizona.edu | ||
| Kevin MacDow | macdow@email.arizona.edu | ||
| Brian Heinze | heinze@email.arizona.edu |
Meetings
Lab Work: As needed, various times, various places
Next Meeting: Mon 7/10 in Shantz 440 at 5:00 pm
Resources
Local Resources
- [http://igem.engr.arizona.edu/phpBB2/ Team Forum]
Articles and References
Related Projects and Links
Projects
Our project ideas that we considered are located at Project Ideas.
We also maintain a forum for internal team communication. This is available at our [http://igem.engr.arizona.edu/phpBB2/ Team Forum].
The "Water Color" system is the project that we are building. As of now, we will be focusing our attention on building this design. We want to start with a system that is not as complex and that is somewhat straightforward to build. So that way, we can learn while we build. We wish to add complexity later, time and resources permitting, after we have made what is already designed.
Project Details
The current name of our project is "Water Color." It is a system that selectively expresses one of three florescence proteins. Each of the three florescence proteins will be expressed in the presence of a unique inducer. Each florescent protein will be controlled by a unique repressed promoter. Thus we will have the expression of three flourescent proteins activated by the presence of there respective inducers.
The idea of our project is to have a media with these cells on it so that each cell will be individually activated to shown a certain "color" (in actuallity, express one florescent protein, which may or may not look unique). Thus the media is able to dispaly an image. A further idea, to be implemented later, is to have the ability to "erase" the image. This would be accomplished by repressing all three promoters.
All the requisite parts have been identified from the registry, and will be built together. (More detail on the specific part numbers and a diagram will be added later)
A flowchart of the parts construction is completed at Parts Schedule
We are currently in Phase III of the construction (much to our plesant surprise). This has not taken too long to reach this far, therefore, we will have time to add improvements to the design.
Visualization
One hurdle to overcome is how should we visualize the image. We know that two of the flourescent proteins look very similar by the naked eye, even though they produce light of different wavelengths. Ideas that we have to better visualize the image include:
- Making three plates (each one color) for each image and digitally adding color
- Use light filters to distinguish the proteins
- View under a microscope
Placing the inducer(s)
After the challenges of the first aspect of the project are overcome, more mechanical challenges still exist. For example: How to place the inducers?, or What scale should the image be?, or Are any optical techniques needed to fully visualize the image?
Inkjet Printer
The first idea to place the inducers on the media is to use an injet printer. The printer could print solutions of inducers on a thin sheet which can be placed onto the media to put the inducers in contact with the cells. Issues that arrise are:
- The size of molecules and the aperature of the jet
- The fluid properties of the solution (e.g. viscosity) should match ink
- The sheet needs to effectively transfer the solutions to the media without mixing of regions
Rapid Prototyping Mold
Digital images could be parsed into its three separate colors. The area were there is color is then cut into a block (not in actuality, it is RP'ed in one step). The block is then used to cast a PDMS mold that will be used as a stamp to place the inducers on the plate of cells.
PDMS Mold
Similar to the above idea, a PDMS mold with microfluidic channels is made so that a liquid (a solution of inducer) is able to be selectively placed on the plate of cells.
Characterization
Sequencing
Selection
Imaging
Last Steps
Issues
Currently we are having issues distinguishing the flourescence. Cells with the plasmid alone show up brighter under a flourescent scope than wild type cells. However, once the cells with our plasmid are grown with the inducer, they are only marginally brighter than the cells that were not grown up in inducer. This poses a problem because it is difficult to distinguish between the "on" and "off" states for a certain flourescence.
Photos
Team Photo:
